Site Technology

Clinical Conductor CTMS

Clinical Trial Management System (CTMS)

Trusted by Clinical Research Leaders

$
Recovered in unbilled payments

Why Clinical Conductor?

Boost Profitability

Run your research as a business with budgeting, billing, and reporting tools designed specifically for clinical research sites. 

Enhance Visibility 

Utilize advanced reporting and analytics to help measure your success, optimize operational workflows, and gain visibility into finances. 

Streamline Enrollment 

Use patient recruitment and enrollment tools to optimize your recruitment tasks, track progress in detail, and reach more participants in less time. 

Improve Participant Engagement

Leverage add-on modules to easily reach your participants, reduce no- shows, and facilitate engagement throughout the study.

Connect Your Technology 

Integrate with Advarra eReg or eSource + EDC, or use Clinical Conductor’s API to connect with other platforms throughout your organization.

Enhance the Patient Experience 

Optional remote workflow enablement, communication, and payment modules to help you keep patients engaged and improve their overall trial experience. 

CC Text
Learn more about CCPay

Make Participant and Caregiver Payments Easier  

Enhance the Patient Experience 

CC Text

Stay Connected With Participant-centric, Two-way Text Messaging 

Make Participant and Caregiver Payments Easier  

Connect Your Clinical Research Technology 

eReg

Save money, improve efficiency, and ensure regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory management and eConsent workflows for any size research site.

eSource + EDC

Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant eSource + EDC system integrated with Clinical Conductor CTMS. 

Connect Your Clinical Research Technology 

eReg

Save money, improve efficiency, and ensure regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory management and eConsent workflows for any size research site.

eSource + EDC

Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant eSource + EDC system integrated with Clinical Conductor CTMS. 

Featured Content

Secure Your Data in a Next-generation Cloud Platform 

Secure Your Data in a Next-generation Cloud Platform 

Collaborate and Drive Clinical Research Forward

Advarra welcomes technology customers to a robust network of the nation’s leading clinical research professionals sharing best practices and addressing current challenges. The Onsemble Community allows researchers to collaborate with colleagues while shaping the industry and the technologies we use every day. When we work together, we can all move clinical research forward. 

Scroll to Top